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"37000-512-02" National Drug Code (NDC)
Crest Sensitivity 1 TUBE in 1 CARTON (37000-512-02) > 24 g in 1 TUBE (37000-512-01)
(Procter & Gamble Manufacturing Company)
NDC Code
37000-512-02
Package Description
1 TUBE in 1 CARTON (37000-512-02) > 24 g in 1 TUBE (37000-512-01)
Product NDC
37000-512
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Crest Sensitivity
Proprietary Name Suffix
Clinical Sensitivity Relief
Non-Proprietary Name
Potassium Nitrate And Sodium Fluoride
Dosage Form
PASTE, DENTIFRICE
Usage
DENTAL
Start Marketing Date
20100830
Marketing Category Name
OTC MONOGRAPH FINAL
Application Number
part355
Manufacturer
Procter & Gamble Manufacturing Company
Substance Name
POTASSIUM NITRATE; SODIUM FLUORIDE
Strength
.05; 243
Strength Unit
g/g; g/g
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37000-512-02